RESUMO
Okadaic acid (OA) and the related dinophysistoxins are isolated from dinoflagellates of the genus Prorocentrum and Dinophysis. Bacteria of the Roseobacter group have been associated with okadaic acid producing dinoflagellates and have been previously implicated in OA production. Analysis of 16S rRNA libraries reveals that Roseobacter are the most abundant bacteria associated with OA producing dinoflagellates of the genus Prorocentrum and are not found in association with non-toxic dinoflagellates. While some polyketide synthase (PKS) genes form a highly supported Prorocentrum clade, most appear to be bacterial, but unrelated to Roseobacter or Alpha-Proteobacterial PKSs or those derived from other Alveolates Karenia brevis or Crytosporidium parvum.
Assuntos
Dinoflagellida/metabolismo , Ácido Okadáico/metabolismo , Policetídeo Sintases/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Dinoflagellida/enzimologia , Dinoflagellida/genética , Filogenia , RNA Ribossômico 16S/genética , Roseobacter/metabolismo , Alinhamento de SequênciaRESUMO
Three polyprenylated phloroglucinol derivatives, namely erectquione A, B, and C, were isolated from Hypericum erectum. Their structures were established using extensive spectral methods.
Assuntos
Clusiaceae/química , Floroglucinol/análogos & derivados , Floroglucinol/química , Modelos Moleculares , Estrutura Molecular , Floroglucinol/isolamento & purificaçãoRESUMO
From the leaves of Mallotus apelta two new benzopyran compounds (1,2) were obtained and their structures were determined using spectroscopic methods.
Assuntos
Benzopiranos/isolamento & purificação , Mallotus (Planta)/química , Benzopiranos/química , Medicina Tradicional Chinesa , Análise EspectralRESUMO
The hepatotoxin okadaic acid (OA) was incubated with nine human recombinant cytochrome P450s (1A1, 1A2, 2C8, 2C9, 2C19, 2D6, 2E1, 3A4 and 3A5). Both CYP3A4 and CYP3A5 converted OA to a mixture of the same four metabolites, but incubation with CYP3A4 resulted in higher levels of conversion. Michaelis-Menten parameters, K(m) (73.4 microM) and V(max) (7.23 nmol of metabolitesnmol(-1)min(-1)) for CYP3A4 were calculated by analyzing double-reciprocal plots. LC-MS(n) analysis and chemical interconversion indicate that metabolites 2 and 3 are the 11S-hydroxy and 11R-hydroxy okadaic acid respectively, while metabolite 4 is 11-oxo okadaic acid. LC-MS(n) analysis of metabolite 1 shows a molecular ion which corresponds to an addition of 16 amu to OA, also suggesting hydroxylation, but the specific site has not been identified. The same four metabolites were produced upon incubation of okadaic acid with pooled human liver microsomes. This transformation could be completely inhibited with ketokonazole, and inhibitor of the CYP3A family of enzymes. The metabolites were determined to be only slightly less potent inhibitors of serine threonine protein phosphatase 2A (PP2A) when compared to OA. As PP2A is the principle molecular target for OA, these oxidative transformations may not effectively detoxify OA.
Assuntos
Doença Hepática Induzida por Substâncias e Drogas/enzimologia , Citocromo P-450 CYP3A/metabolismo , Inibidores Enzimáticos/metabolismo , Ácido Okadáico/metabolismo , Biotransformação , Cromatografia Líquida de Alta Pressão , Cromatografia por Troca Iônica , Inibidores do Citocromo P-450 CYP3A , Inibidores Enzimáticos/farmacologia , Humanos , Técnicas In Vitro , Cinética , Fígado/enzimologia , Espectrometria de Massas , Microssomos Hepáticos/enzimologia , Ácido Okadáico/farmacologia , Oxirredução , Proteína Fosfatase 2/antagonistas & inibidores , Proteínas Recombinantes/metabolismo , Espectrometria de Massas por Ionização por Electrospray , Xenobióticos/metabolismoRESUMO
Four metabolites were identified upon incubation of brevetoxin (PbTx-2) with human liver microsomes. Chemical transformation of PbTx-2 confirmed the structures of three known metabolites BTX-B5, PbTx-9 and 41, 43-dihydro-BTX-B5 and a previously unknown metabolite, 41, 43-dihydro-PbTx-2. These metabolites were also observed upon incubation of PbTx-2 with nine human recombinant cytochrome P450s (1A1, 1A2, 2C8, 2C9, 2C19, 2D6, 2E1, 3A4 and 3A5). Cytochrome P450 3A4 produced oxidized metabolites while other CYPs generated the reduced products.
Assuntos
Toxinas Marinhas/metabolismo , Sistema Enzimático do Citocromo P-450/química , Sistema Enzimático do Citocromo P-450/metabolismo , Humanos , Toxinas Marinhas/química , Microssomos Hepáticos/metabolismo , Oxocinas , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismoRESUMO
Extracts of fifty-seven newly isolated strains of dinoflagellates and raphidophytes were screened for protein phosphatase (PP2A) inhibition. Five strains, identified by rDNA sequence analysis as Prorocentrum rhathymum, tested positive and the presence of okadaic acid was confirmed in one strain by HPLC-MS/MS and by HPLC with fluorescence detection and HPLC-MS of the okadaic acid ADAM derivative. Quantitation of the ADAM derivative indicated that the concentration of okadaic acid in the culture medium is 0.153 microg/L.
Assuntos
Dinoflagellida/metabolismo , Ácido Okadáico/metabolismo , Sequência de Aminoácidos , Cromatografia Líquida de Alta Pressão , DNA/análise , DNA/genética , Bases de Dados Genéticas , Dinoflagellida/genética , Florida , Espectrometria de Massas , Dados de Sequência Molecular , Ácido Okadáico/farmacologia , Proteína Fosfatase 2/antagonistas & inibidores , Espectrometria de FluorescênciaRESUMO
The isolation and structure elucidation of two cyclic peptides, pahayokolides A (1) and B (2), is described. Structural features determined for these compounds include a pendent N-acetyl-N-methyl leucine, both E- and Z-dehydrobutyrines, a homophenylalanine, and an unusual polyhydroxy amino acid that is most likely of mixed polyketide synthase/nonribosomal peptide synthase origin. These peptides were purified from a new species of cyanobacteria of the genus Lyngbya, which was isolated from a periphyton mat from the Florida Everglades.
Assuntos
Cianobactérias/química , Toxinas de Lyngbya/química , Peptídeos Cíclicos/química , Florida , Água Doce , Estrutura MolecularRESUMO
The root of Stellera chamaejasme L. is a traditional Chinese herb termed Rui Xiang Lang Du and has been used to treat solid tumors, tuberculosis and psoriasis. Exactly how S. chamaejasme L. regulates cellular responses remains unclear. We examined four biflavonoids isolated from S. chamaejasme L., including isochamaejasmin, two of its stereo-isomers and a methyl derivative, in functional assays originally designed to screen ligands for the G protein-coupled formyl peptide receptor-like 1 (FPRL1). Isochamaejasmin was found to induce the expression of a nuclear factor (NF)-kappaB-directed reporter gene in transfected HeLa cells with an EC50 of 3.23 microM, independently of FPRL1. The isochamaejasmin-stimulated NF-kappaB reporter activity was accompanied by nuclear translocation of NF-kappaB proteins and was blocked by a dominant-negative construct of IkappaBalpha. Isochamaejasmin also induced time-dependent phosphorylation of the mitogen-activated protein kinases extracellular signal-regulated kinase 1/2 and p38, and a novel protein kinase C (PKCdelta). Likewise, inhibition of these kinases with the respective pharmacological inhibitors significantly reduced the isochamaejasmin-stimulated NF-kappaB activation. It is noteworthy that the two stereoisomers and the methyl derivative did not induce detectable activation of NF-kappaB and were more cytotoxic than isochamaejasmin, which could partially rescue cycloheximide-induced apoptosis. Inhibition of NF-kappaB activation reversed the anti-apoptotic effect of isochamaejasmin. These results provide the first evidence for a potential mechanism of action by S. chamaejasme L., and indicate that structurally similar compounds derived from S. chamaejasme L. may have different pharmacological properties.